tert-butyl 4-((3-(cyclopropylmethoxy)-5-methoxybenzamido)methyl)piperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-((3-(cyclopropylmethoxy)-5-methoxybenzamido)methyl)piperidine-1-carboxylate
CAS No.:1428582-13-1
Molecular Formula:C₂₃H₃₄N₂O₅
Molecular Weight:418.533
Hs Code.:

Synonyms:tert-butyl 4-((3-(cyclopropylmethoxy)-5-methoxybenzamido)methyl)piperidine-1-carboxylate

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Chemical Property of tert-butyl 4-((3-(cyclopropylmethoxy)-5-methoxybenzamido)methyl)piperidine-1-carboxylate

Chemical Property:

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Technology Process of tert-butyl 4-((3-(cyclopropylmethoxy)-5-methoxybenzamido)methyl)piperidine-1-carboxylate

There total 4 articles about tert-butyl 4-((3-(cyclopropylmethoxy)-5-methoxybenzamido)methyl)piperidine-1-carboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 1369862-57-6
3-(cyclopropylmethoxy)-5-methoxybenzoic acid

: 144222-22-0
tert-butyl 4-(aminomethyl)piperidine-1-carboxylate

: 1428582-13-1
tert-butyl 4-((3-(cyclopropylmethoxy)-5-methoxybenzamido)methyl)piperidine-1-carboxylate

Guidance literature:: 3-(cyclopropylmethoxy)-5-methoxybenzoic acid; tert-butyl 4-(aminomethyl)piperidine-1-carboxylate; With N-ethyl-N,N-diisopropylamine; In dichloromethane; for 0.25h;

With HATU; In dichloromethane; at 20 ℃; for 2h;

Reference yield:

: 2150-44-9
1-carbomethoxy-3,5-dihydroxybenzene

: 1428582-13-1
tert-butyl 4-((3-(cyclopropylmethoxy)-5-methoxybenzamido)methyl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: sulfuric acid / 4 h / Reflux

2.1: potassium carbonate / acetonitrile / 5 h / 70 - 80 °C

3.1: lithium hydroxide monohydrate / methanol; water / 3 h / 20 °C

4.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 0.25 h

4.2: 2 h / 20 °C

With lithium hydroxide monohydrate; sulfuric acid; potassium carbonate; N-ethyl-N,N-diisopropylamine; In methanol; dichloromethane; water; acetonitrile;

Reference yield:

: 19520-74-2
3-hydroxy-5-methoxy-benzoic acid methyl ester

: 1428582-13-1
tert-butyl 4-((3-(cyclopropylmethoxy)-5-methoxybenzamido)methyl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium carbonate / acetonitrile / 5 h / 70 - 80 °C

2.1: lithium hydroxide monohydrate / methanol; water / 3 h / 20 °C

3.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 0.25 h

3.2: 2 h / 20 °C

With lithium hydroxide monohydrate; potassium carbonate; N-ethyl-N,N-diisopropylamine; In methanol; dichloromethane; water; acetonitrile;